1039136-82-7

Upstream product

• 201230-82-2 carbon monoxide 
• 1651-41-8 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecan-1-ol 
• 1039136-57-6 2-(trimethylsilyl)ethyl 3,3-difluoro-2-[(4-methoxyphenyl)imino]-5-hexenoate 
• 200112-75-0 3-(perfluorooctyl)propyl iodide 

Downstream Products

• 1071528-21-6 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl 3,3-difluoro-2-(4-methoxyphenyl)amino-2-(2-methylallyl)-5-hexenoate 
• 1071528-15-8 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl 2-allyl-3,3-difluoro-2-(4-methoxyphenyl)amino-5-hexenoate 
• 1071528-23-8 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl 2-(1,1-difluorobut-3-enyl)-1-(4-methoxyphenyl)-4-methylene-5-oxopyrrolidine-2-carboxylate 

Relevant academic research and scientific papers

Solution-, solid-phase, and fluorous synthesis of β,β- difluorinated cyclic quaternary a-amino acid derivatives: A comparative study

The diastereoselective synthesis of cyclic β,β-difluorinated α-amino acid derivatives bearing a quaternary stereocenter is described. The process relies on the chemo- and diastereoselective addition of allylic organometallic reagents to fluorinated αimino

Selective formal transesterification of fluorinated 2-(trimethylsilyl)ethyl α-imino esters mediated by TBAF

(Chemical Equation Presented) The scope of the transesterification reaction between β-fluorinated α-imino esters and various electrophiles in the presence of TBAF as fluorine source is described. The reaction is highly selective for alkyl iodides, bromide